cifri annual report 2007- 2008 - Central Institute of Brackishwater ...
cifri annual report 2007- 2008 - Central Institute of Brackishwater ...
cifri annual report 2007- 2008 - Central Institute of Brackishwater ...
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A spectrophotomctric procedure for estimation <strong>of</strong><br />
phenol in bacterial broth culture has becn<br />
The IINA was also used to amplify the mitochoncirial<br />
DNA genes. Scvcral genes were atnplified,<br />
standardized. Standard curve <strong>of</strong> phcnol for C'ytochronie b gene, C'ytochrome oxidnsc II. 16s<br />
photometric cstimation <strong>of</strong> phenol was drawn. Tlirec<br />
bacterial strains wcre examined and were found to<br />
degrade plicnol and pentachlorophcnol. to different<br />
extents.<br />
rKNA gene. The C\~toc*lit-ornc~ h gene :~mpIification<br />
resulted in a a11.lplilication fragmetit <strong>of</strong> 360 bp. This<br />
360 kp DNA fragment fiom P. ticeto, .Y(*tlc~todoll<br />
c.nnc-ila and Gudlisi~t c-/irrpr.cl were seclucnccd.<br />
Strcss metliatctl gcncfic xltcration in fish<br />
Assessment <strong>of</strong> gcnctic changes were investigated in<br />
J'trtt tiu,v ticsro, A'~~~tcrtrot/otr c*trt~c.iln, and Gc~dzi.vi(r<br />
c*kap+cr samples fio~n different locations on the rivcr<br />
Damodar representing tlic uy)strearn reference site with<br />
low pollution. Industrit~l polluted sitc arid downstream<br />
<strong>of</strong>' industrial sitc. 'The 4 RAPD-PCR oligo-dcgcticrate<br />
primers wcrc uscd for amplification <strong>of</strong>'gcnomic DNA.<br />
Each prinier was found to be highly polymorphic and<br />
the number <strong>of</strong> fragments amplified was large. l'hc<br />
RAPD patterns wcrc gct~cr;~tccl for all tlic sarnplcs<br />
collected fiom the above-mentioned locations. Tlicsc<br />
fragment pattenis wcrc then analyzcd for tlic prcscncc<br />
and absence <strong>of</strong>'amplificd bands.<br />
Tahlc 8 : Primer Sequences<br />
Primcrs Sequence 5'- 3' %GC contcnt<br />
i.'ish prolcomics strrdy<br />
'T'issuc proteins viz. scrurn, ~nusclc, lens anti KHC'<br />
mcmbrane <strong>of</strong> fish Ritu ritu wcre sutjcctcd to<br />
proteomic analysis. Ritc~ rittr wcrc collcc~ed fj.0111 tlic<br />
local markets live. Scrull.1, muscle, and lens prolcins<br />
were analyzed by onc-ditncnsional sodium dodecyl<br />
anellis polyilcrylamidc gel electrophoresis ( I -rl (-;I:)<br />
and protcin pr<strong>of</strong>iles werc gcncratcd. 'Tht~s~: tissuc<br />
proteins wcrc also analyzcd by 2-dimvnsional<br />
polyac~ylamidc gcl electrophoresis (2-D GE) fiv<br />
generating protcorric maps.<br />
In the river [lamotfar niusclc ancl lens protcins <strong>of</strong>.4.<br />
.vc~cti~rtlr~rla wcre analyzed by I- and 2- D GE and<br />
protein pr<strong>of</strong>ilcs wcrc gcnel-atcd. Imagc irnalysis is<br />
being carried out.<br />
Protein pr<strong>of</strong>ilc <strong>of</strong> fish mucus was dctcr~~~irrcd tty SDS-<br />
PAGE for idcntifica~ivn <strong>of</strong> antibacterial proteins. Tlic<br />
mctliod is fi~rthcr st;rndal-dizcd for rc~noval <strong>of</strong>'<br />
hindering f'actors like lipid, carboliydlates anrl nonsolublc<br />
protein moieties.<br />
PCR was carricd out in 25 1<br />
reaction mixturc<br />
containing 100 ng DNA, 100 pM <strong>of</strong> decamer primer,<br />
10 mM dNTP mixture (Dynazymc), 10 X PCR bufTer<br />
(Dynazymc), 1.5 mM MgCl, and 0.05 U <strong>of</strong> Xlq<br />
polymerases (Dynazymc).<br />
Fig. 7 : Sl!S-l'.\( ;I I",, I'~-olilc jlcl~tidcs fro~ri<br />
sAlri nillctls <strong>of</strong>'conttx)l fi!,ll